TECHNICAL FIELD
[0001] This invention relates to a process for producing an oxide superconductor. In particular,
this invention relates to the improvement of the process for producing tape-shaped
Re-type (123) superconductor by MOD process which is useful to such as a superconducting
magnet, a superconducting electric power cable and an electric power device.
BACKGROUND ART
[0002] About the oxide superconductor, because that critical temperature (Tc) exceeds the
liquid nitrogen temperature, the applications for such as the superconducting magnet,
the superconducting electric power cable, the electric power device and the device
are expected, and the many studies are reported.
[0003] In order to apply the oxide superconductor to the above-mentioned field, it is necessary
to produce a long wire which has high critical current density (Jc) and high critical
current value (Ic) . On the other hand, in order to obtain a long tape, it is necessary
to form the oxide superconductor onto a metallic tape from the viewpoint of strength
and flexibility. Also, in order to enable use of the oxide superconductor at a practical
level which is equivalent to the metallic superconductor such as Nb
3Sn or Nb
3Al, the Ic value of about 500 A/cm (at 77 K, in self-field) is required.
[0004] Further, in the oxide superconductor, because the superconducting characteristic
changes by its crystal orientation, in order to improve the Jc, it is necessary to
improve the in-plane orientation, and to form the oxide superconductor onto the tape-shaped
substrate. For this reason, the process for forming film which makes the oxide superconductor
grow epitaxially onto the substrate having high in-plane orientation is adopted.
[0005] In this case, in order to improve the Jc, it is necessary to make c-axis of the oxide
superconductor orient perpendicularly to the plane of the substrate and to make its
a-axis (or b-axis) orient in plane in parallel to the plane of the substrate, and
it is necessary to maintain the quantum connectivity of the superconducting state
well. For this reason, by forming the intermediate layer which makes the in-plane
orientation degree and the direction improve onto the metallic substrate which has
the high in-plane orientation, and by using the crystal lattice of this intermediate
layer as the template, making the in-plane orientation degree and the direction of
the crystal of the superconducting layer improve is performed. In addition, in order
to improve the Ic value, it is necessary to thicken the film thickness of the oxide
superconductor which is formed onto the substrate.
[0006] As the process for producing the tape-shaped Re-type oxide superconductor, that is,
as the process for producing ReBa
2Cu
3O
y type oxide superconductor (wherein, Re shows at least more than one kind of element
selected from Y, Nd, Sm, Gd, Eu, Yb, Pt or Ho. Hereinafter called Re-type (123) superconductor.),
MOD process (Metal Organic Deposition Processes) is known.
[0007] This MOD process makes metal organic acid salt decompose thermally. And after coating
the solution that organic impound of metallic component is dissolving uniformly onto
the substrate, by heating this and then by making this decompose, the thin film is
formed onto the substrate. Because this MOD process is non-vacuum process, it is possible
to form the film at low cost and high speed, and because high Jc can be obtained,
there is an advantage which is suitable to produce the long tape-shaped oxide superconducting
wire.
[0008] In MOD process, when making the metal organic acid salt as starting material decompose
thermally, the carbonate of alkali earth metal (such as Ba) is usually formed. However,
in the forming of the oxide superconductor by a solid-phase reaction through this
carbonate, the high temperature heat treatment of 800 °C or more is required. Further,
when forming the thick film, because the nucleation for crystal growth occurs also
from parts other than the interface of the substrate, it is difficult to control the
crystal growth rate. Consequently, there is a problem that it is difficult to obtain
the superconducting film having superior in-plane orientation, that is, high Jc.
[0009] In order to solve the above-mentioned problem in MOD process, as the process for
producing Re-type (123) superconductor without going through the carbonate, recently,
the process for obtaining the superconductor is conducted vigorously by using organic
acid salt containing fluorine (for example, TFA salt: trifluoroacetate) as the starting
material, by performing the heat treatment in a water vapor atmosphere under the control
of the water vapor partial pressure, and by going through decomposition of fluoride.
[0010] In MOD process which uses this TFA salt as the starting material, by reaction between
amorphous precursor containing fluorine which is obtained after calcination of the
coating film and water vapor, the superconductor grows epitaxially from the interface
of the substrate by forming the liquid phase caused by HF at the interface that the
superconducting film grows while generating HF gas. In this case, because it is possible
to control the decomposition rate of the fluoride by water vapor partial pressure
in heat treatment, the crystal growth rate of the superconductor can be controlled.
Consequently, it is possible to produce the superconducting film having superior in-plane
orientation. Further, in this process, it is possible to make the Re-type (123) superconductor
grow epitaxially from the upper surface of the substrate at comparatively low temperature.
[0011] Heretofore, in order to enable the thick film and the high speed calcination process,
the mass generation of HF gas in the calcination process is prevented by using the
solution which mixed the TFA salt of Y and Ba and the naphthenate of Cu as the starting
materials into the organic solvent at the molar ratio of Y : Ba : Cu = 1 : 2 : 3.
[0012] As described above, when the tape-shaped oxide superconductor is produced by MOD
process, thickening the film to improve the Ic value is essential for practical application.
For accomplishing the forming of the thick film by MOD process when the starting material
is TFA salt, there are thoughts of increasing the viscosity of the material solution
containing TFA salt and of thickening the coating film. However, when the thickness
of the coating film per once becomes thick, because gas yield of HF and CO
2 by decomposition in heat treatment increases, the phenomenon that the coating film
is scattered in calcination occurs. Consequently, it is difficult to produce the thick
film of the tape-shaped oxide superconductor having high characteristic.
[0013] In order to produce the thick film of the superconductor, there is a thought that
it is possible to thicken the calcination film by repeating the steps of the coating
of the material and the calcination. However, in the above-mentioned calcination heat-treatment
method of conventional technology, because the temperature-increasing rate which affects
the decomposition rate of the metal organic acid salt in the calcination heat-treatment
is fast, the decomposition of the metal organic acid salt including TFA salt is insufficient.
Consequently, there is a tendency that the solvent or the organic acid salt remains
in the film of the oxide superconductor precursor which is obtained by the calcination.
Therefore, at the time of temperature rising of the subsequent heat treatment for
crystallization, the remaining organic acid salt such as fluoride decomposes rapidly,
and the bumping evidences, the extraneous materials, the pores, etc. are generated
in the film. Further, the stress is generated in the film by the volume shrinkage
when the calcination film decomposes and the crystal of YBCO is formed, and the cracks
that the bumping evidences, the extraneous materials, the pores, etc. become the starting
point are generated.
[0014] This tendency becomes remarkable when the film of the oxide superconductor precursor
of multilayer structure is formed and when thickening the film by repeating the coating
and the calcination heat-treatment. Consequently, the cracks remain in the state as
it is when the obtained thick film of the precursor is crystallized, and when the
superconducting film is obtained. Therefore, because the current pathway is blocked
when applying current, the Jc characteristic deteriorates remarkably.
[0015] In order to solve these problems, by controlling the temperature-increasing rate
in the calcination heat-treatment, and then by making the metal organic acid salt
recompose sufficiently, the method to accomplish the thick film and high Jc is known
(for example, refer to Patent document No.1).
[0016] Besides, by controlling the calcination heat-treatment at the time of the heat treatment
of the oxide superconductor precursor formed onto the substrate, and/or, by controlling
the water vapor partial pressure of introduced gas in the atmosphere of the crystallization
heat-treatment, the process for producing thick-film tape-shaped oxide superconductor
having high orientation and high Jc is known (for example, refer to Patent document
No.2).
[0017]
Patent document No.1: Japanese Patent Publication No.2003-300726
Patent document No.2: Japanese Patent Publication No.2003-34527
DISCLOSURE OF THE INVENTION
PROBLEM TO BE SOLVED BY THE INTENTION
[0018] However, in the above-mentioned process which controls the temperature-increasing
rate in the calcination heat-treatment, or, in the processes which control the calcination
heat-treatment and/or the water vapor partial pressure of introduced gas in the atmosphere
of the crystallization heat-treatment, although thickening the film was achieved than
before, the film thickness was limited to approximately 1.0µm. And the cracks are
generated when the film thickness reached approximately 1. 5µm even in the improved
process of the crystallization heat-treatment. Therefore, it was difficult to obtain
the thick film having high Jc and Ic values.
[0019] This invention was conducted based on the knowledge that the deterioration of Jc
associated with thickening the film or the low Ic value than the prospective value
are caused by not only generation of the cracks but also the deterioration of the
electric connectivity. And this invention aims to provide the process for producing
the thick film tape-shaped Re-type (123) superconductor having high Jc and Ic values
by removing or preventing these causes of the generation of the cracks and the deterioration
of the electric connectivity of the crystal grain boundary.
MEANS FOR SOLVING THE PROBLEMS
[0020] In order to solve the above-mentioned problems, in the process for producing tape-shaped
Re-type (123) superconductor of this invention, in the process for producing tape-shaped
Re-type (123) superconductor by giving the calcination heat-treatment after coating
the raw material solution including metal elements which compose the Re-type (123)
superconductor (ReBa
2Cu
3O
y, wherein, Re is at least more than one kind of element selected from Y, Nd, Sm, Gd,
Eu, Yb, Pr or Ho) onto the substrate, and subsequently giving the heat treatment for
producing the superconductor, the raw material solution of the molar ratio of Ba of
the range of X < 2 when the molar ratio of Re, Ba and Cu in above-mentioned raw material
solution is Re : Ba : Cu = 1 : X : 3 is used.
[0021] In this case, in order to obtain high Jc and Ic values, it is preferable that the
molar ration of Ba in the raw material solution is in the range of 1.0 ≦ X ≦ 1.8,
more preferably, the molar ration of Ba in the raw material solution is in the range
of 1.3 ≦ X ≦ 1.7.
EFEECT OF THE INVENTION
[0022] In this invention, by making the molar ratio of Ba of the superconductor reduce than
the standard molar ratio (Y : Ba : Cu = 1 : 2 : 3), the segregation of Ba can be prevented.
Consequently, by presenting the precipitation of the impurities of Ba base in the
crystal grain boundary, the generation of the cracks is prevented and the electric
connectivity among the crystal grains improves, and the tape-shaped Re-type (123)
superconductor which has high Jc and Ic values can be produced. Further, by forming
the superconducting film by MOD process, the tape-shaped Re-type (123) superconductor
which has high speed, uniform thick film and excellent superconducting characteristic
can be produced easily.
BRIEF DESCRIPTION OF THE FIGURES
[0023] [Fig.1] The drawing which shows the cross section perpendicular to the axial direction
of the tape of the tape-shaped Re-type (123) superconductor which is produced by this
invention. BEST MODE FOR CARRYING OUT THE INVENTION
[0024] As described above, this invention has the feature that the molar ratio of the tape-shaped
Re-type (123) superconductor, that is, the molar ratio of Ba of ReBa
2Cu
3O
y superconductor is reduced than the standard molar ratio.
[0025] Fig.1 shows the perpendicular cross section to the axial direction of the tape of
the tape-shaped Re-type (123) superconductor which is produced by this invention.
The tape-shaped Re-type (123) superconductor 10 has the cross section structure that
the stabilized layer 3 comprising the Re-type (123) superconductor 2 and Ag etc. is
formed on the surface of the tape-shaped substrate 1.
[0026] As the substrate 1, the biaxially-oriented substrate 1a is used. As shown in Fig.1,
the composite substrate of which the high oriented intermediate layer comprising one
or more layers, for example, the first intermediate layer 1b and the second intermediate
layer 1c, is formed on the biaxially-oriented substrate 1a comprising such as the
Ni-based alloy is preferable.
[0027] The above-described intermediate layer has the function as the buffer layer and is
arranged to suppress the reaction with the superconducting layer, to prevent the deterioration
of the superconducting characteristic, and to maintain the consistency with the superconducting
layer.
[0028] As the above-described intermediate layer, for example, A
2Zr
2O
7 film (wherein, A is one kind of any one of Ce, Gd or Sm) which is formed by MOD process
is used as the first intermediate layer, and CeO
2 film or Ce-Gd-O film which is formed by MOD process, CVD process or pulse-deposition
technique is used as the second intermediate layer.
[0029] The Re-type (123) superconductor 2 is formed by MOD process. As the raw material
solution, it is preferable to use the mixed solution which includes the organic solvent
and any one or more kinds of trifluoroacetate, naphthenate, octylic acid salt, neodecanoic
acid salt, isononanoic acid salt.
[0030] In this case, the raw material solution comprising the mixed solution of Y-TFA salt
(trifluoroacetate) including the organic solvent and fluorine, Ba-TFA salt and naphthenate
of Cu can be used.
[0031] As described above, from the viewpoint of improvement of the superconducting characteristic,
when thickening the film, the generation of cracks becomes a problem. These applicants
investigated the cause that the cracks generated when thickening the film. And these
applicants filed process for producing thick-film tape-shaped Re-type (123) superconductor
(application No.
2005-360788) which discharged the remained organic component or the residual fluoride in the
calcination before reaching the crystallization temperature of YBCO (YBa
2Cu
3O
Y) by giving the intermediate heat-treatment at low temperature than the heat-treatment
temperature for forming the superconductor between the calcination heat-treatment
and the heat-treatment for forming the superconductor and prevented the generation
of cracks.
[0032] According to the knowledge of this time, in the features of MOD process whose starting
material is TFA salt, the superconductor is formed by reaction between the precursor
including fluorine and the water vapor in the crystallization heat-treatment, and
the crystal growth rate can be controlled by the water vapor partial pressure, and
the growth rate of YBCO superconducting phase increases along with the rise of the
water vapor partial pressure. However, Jc of the YBCO superconducting film decreases
rapidly when exceeding the critical water vapor partial pressure by generation of
cracks or formation of pores in YBCO superconducting film.
[0033] Besides, it is thought that the rough composition containing many pores which are
formed after rapid decomposition and desorption of the organic component when the
temperature rises in the crystallization heat-treatment becomes the starting points
of the local strain and stress when the volume of the film along with the subsequent
formation of YBCO phase shrinks, and this becomes the cause of the generation of the
cracks.
[0034] However, as the result of the subsequent study, these applicants reasoned that the
deterioration of Jc or Ic values did not originate due to only generation of cracks,
and that the starting points of the local strain and stress which is the cause of
the generation of cracks did not originate due to only rough composition containing
many pores.
[0035] That is, among the metallic elements which constitute the Re-type (123) superconductor,
depending on the condition of the calcination process, especially Ba does not disperse
uniformly in the calcination film and tends to produce the segregation, and Ba becomes
excess locally in the domain where this segregation occurs. Therefore, Ba impurities
such as BaCeO
3 are formed in addition to the Re-type (123) superconductor. In many cases, this Ba
impurities precipitate in the grain boundaries. Consequently, the impurities which
are dielectric substance intervene in the grain boundaries, and the electric connectivity
among the crystal grains are spoiled, in addition, it becomes one of factors which
induce the generation of cracks, and as a result, it is thought that these become
the cause that Jc or Ic values decrease.
[0036] Based on such a thought, in this invention, especially only molar ratio of Ba among
the metallic elements which constitute the Re-type (123) superconductor is lowered
than the standard molar ratio. In this invention, by lowering the molar ratio of Ba,
the segregation of Ba is prevented, and the precipitation of the impurities of Ba
base is prevented in the crystal grain boundary. Consequently, it is thought that
the generation of cracks is prevented, the electric connectivity among the grain boundaries
improves, and Jc which is defined by the conducting current improves.
[0037] Hereinafter, the embodiments of this invention are explained. Embodiments
Embodiment 1
[0038] As the substrate, the composite substrate that the first intermediate layer comprising
Gd
2Zr
2O
7 of 0.7 µm thickness and the second intermediate layer comprising CeO
2 of 0.4 µm thickness were formed in sequence onto the hastelloy tape was used. Δφ
of the second intermediate layer CeO
2 in this case was 4.1° .
[0039] Meanwhile, trifluoroacetate of Y (Y-TFA), trifluoroacetate of Ba (Ba-TFA) and naphthenate
of Cu were mixed so that the molar ratio of Y : Ba : Cu became 1 : 1.5 : 3, and they
were dissolved into 2-octanone so that the metallic content became the concentration
of 1.2 mol/liter, and thereby, the raw material solution was prepared. The viscosity
of this raw material solution was 79.6 cP.
[0040] The raw material solution was coated onto the above-described substrate at the conditions
of the rotation speed of 2500 rpm and the coating time of 60 sec by spin-coat method,
and then the calcination heat-treatment was given. The calcination heat-treatment
was given by cooling the furnace after heating till the maximum heating temperature
(Tmax) of 500 °C in oxygen gas atmosphere of the water vapor partial pressure of 2.5
% at the rate of temperature increase of 2 °C/min.
[0041] After above-mentioned calcination heat-treatment, the superconducting film was formed
onto the substrate by giving the heat-treatment for forming the superconductor (baking).
This baking was heated till the maximum baking-temperature of 760 °C in argon gas
atmosphere of the water vapor partial pressure of 13.5 % (water vapor introducing
temperature: 450 °C) and the oxygen partial pressure of 0.1 % at the rate of temperature
increase of 5 °C/min and held for 200 minutes at this temperature, after then, this
baking was given by cooling the furnace.
[0042] The film thickness of the tape-shaped Re-type (123) superconductor which was produced
by the above-mentioned process was 1.64 µm. And in the results of measured critical
current density and critical current, the results of Jc = 3.20 MA/cm
2 and Ic = 525 A/cm were obtained.
[0043] Besides, in the measured results by X-ray diffraction about the superconducting film
which was obtained by this means, the values of the peak value of (005) face of YBCO
(YBa
2Cu
3O
Y) = 189751 cps, Δφ = 4.12 deg. , Δω = 1. 59 deg., and ∫ω = 38775 were obtained.
Embodiment 2
[0044] The same composite substrate as Embodiment 1 was used, and trifluoroacetate of Y
(Y-TFA), trifluoroacetate of Ba (Ba-TFA) and naphthenate of Cu were mixed so that
the molar ratio of Y : Ba : Cu became 1 : 1.8 : 3, and they were dissolved into 2-octanone
so that the metallic content became the concentration of 1.2 mol/liter, and thereby,
the raw material solution was prepared. The viscosity of this raw material solution
was 78.3 cP.
[0045] The raw material solution was coated onto the above-described substrate by the same
method as Embodiment 1, and then the superconducting film was formed onto the substrate
by giving the calcination heat-treatment and the heat-treatment for forming the superconductor
(baking).
[0046] The film thickness of the tape-shaped Re-type (123) superconductor which was produced
by the above-mentioned process was 1. 5 µm. And in the results of measured critical
current density and critical current, the results of Jc = 2.13 MA/cm
2 and Ic = 320 A/cm were obtained.
[0047] Besides, in the measured results by X-ray diffraction about the superconducting
film which was obtained by this means, the values of the peak value of (005) face
of YBCO (YBa
2Cu
3O
Y) = 182099 cps, Δφ = 4.31 deg. , Δω = 1. 46 deg., and ∫ω = 38545 were obtained.
Embodiment 3
[0048] The same composite substrate as Embodiment 1 was used, and trifluoroacetate of Y
(Y-TFA), trifluoroacetate of Ba (Ba-TFA) and naphthenate of Cu were mixed so that
the molar ratio of Y : Ba : Cu became 1 : 1.0 : 3, and they were dissolved into 2-octanone
so that the metallic content became the concentration of 1.2 mol/liter, and thereby,
the raw material solution was prepared. The viscosity of this raw material solution
was 79.7 cP.
[0049] The raw material solution was coated onto the above-described substrate by the same
method as Embodiment 1, and then the superconducting film was formed onto the substrate
by giving the calcination heat-treatment and the heat-treatment for forming the superconductor
(baking).
[0050] The film thickness of the tape-shaped Re-type (123) superconductor which was produced
by the above-mentioned process was 1.61 µm. And in the results of measured critical
current density and critical current, the results of Jc = 1.74 NA/cm
2 and Ic = 280 A/cm were obtained.
[0051] Besides, in the measured results by X-ray diffraction about the superconducting film
which was obtained by this means, the values of the peak value of (005) face of YBCO
(YBa
2Cu
3O
Y) = 181121 cps, Δφ = 4.33 deg. , Δω = 1.58 deg., and ∫ω = 37639 were obtained.
Comparative example 1
[0052] The same composite substrate as Embodiment 1 was used, and trifluoroacetate of Y
(Y-TFA), trifluoroacetate of Ba (Ba-TFA) and naphthenate of Cu were mixed so that
the molar ratio of Y : Ba : Cu became 1 : 2.0 : 3 (standard composition), and they
were dissolved into 2-octanone so that the metallic content became the concentration
of 1.2 mol/liter, and thereby, the raw material solution was prepared. The viscosity
of this raw material solution was 70.7 cP.
[0053] The raw material solution was coated onto the above-described substrate by the same
method as Embodiment 1, and then the superconducting film was formed onto the substrate
by giving the calcination heat-treatment and the heat-treatment for forming the superconductor
(baking).
[0054] The film thickness of the tape-shaped Re-type (123) superconductor, which was produced
by the above-mentioned process was 1.19 µm. And in the results of measured critical
current density and critical current, the results of Jc = 2058 MA/cm
2 and Ic = 307 A/cm were obtained.
[0055] Besides, in the measured results by X-ray diffraction about the superconducting film
which was obtained by this means, the values of the peak value of (005) face of YBCO
(YBa
2Cu
3O
Y) = 179086 cps, Δφ = 4.12 deg. , Δω = 1. 47 deg., and ∫ω = 20902 were obtained.
Comparative example 2
[0056] The same composite substrate as Embodiment 1 was used, and trifluoroacetate of Y
(Y-TFA), trifluoroacetate of Ba (Ba-TFA) and naphthenate of Cu were mixed so that
the molar ratio of Y : Ba : Cu became 1 : 2.2 : 3, and they were dissolved into 2-octanone
so that the metallic content became the concentration of 1.2 mol/liter, and thereby,
the raw material solution was prepared. The viscosity of this raw material solution
was 70.7 cP.
[0057] The raw material solution was coated onto the above-described substrate by the same
method as Embodiment 1, and then the superconducting film was formed onto the substrate
by giving the calcination heat-treatment and the heat-treatment for forming the superconductor
(baking) .
[0058] The film thickness of the tape-shaped Re-type (123) superconductor which was produced
by the above-mentioned process was 1.63 µm. And in the results of measured critical
current density and critical current, the results of Jc = 1.50 MA/cm
2 and Ic = 245 A/cm were obtained.
[0059] Besides, in the measured results by X-ray diffraction about the superconducting film
which was obtained by this means, the values of the peak value of (005) face of YBCO
(YBa
2Cu
3O
Y) = 158745 cps, Δφ = 4.23 deg. , Δω = 1.56 deg., and ∫ω = 37456 were obtained.
Comparative example 3
[0060] The same composite substrate as Embodiment 1 was used, and trifluoroacetate of Y
(Y-TFA), trifluoroacetate of Ba (Ba-TFA) and naphthenate of Cu were mixed so that
the molar ratio of Y : Ba : Cu became 1 : 2.5 : 3, and they were dissolved into 2-octanone
so that the metallic content became the concentration of 1.2 mol/liter, and thereby,
the raw material solution was prepared. The viscosity of this raw material solution
was 60.5 cP.
[0061] The raw material solution was coated onto the above-described substrate by the same
method as Embodiment 1, and then the superconducting film was formed onto the substrate
by giving the calcination heat-treatment and the heat-treatment for forming the superconductor
(baking).
[0062] The film thickness of the tape-shaped Re-type (123) superconductor, which was produced
by the above-mentioned process was 1.43 µm. And in the results of measured critical
current density and critical current, the results of Jc = 1.01 MA/cm
2 and Ic = 144 A/cm were obtained.
[0063] Besides, in the measured results by X-ray diffraction about the superconducting film
which was obtained by this means, the values of the peak value of (005) face of YBCO
(YBa
2Cu
3O
Y) = 141528 cps, Δφ = 5.29 deg. , Δω = 1. 68 deg., and ∫ω = 17975 were obtained.
[0064] From the above-mentioned embodiments and comparative examples, as the raw material
solution when the tape-shaped Re-type (123) superconductor is produced by MOD process,
by using the raw material solution whose molar ration of Ba is the range of X < 2
or is in the range of 1.0 ≦ x ≦ 1.8 when the molar ratio of Re, Ba and Cu is Re :
Ba : Cu = 1 : X : 3, the superconducting characteristic (Jc value or Ic value) which
is equivalent or more as against the case of making the molar ratio of Ba into the
standard molar ratio can be obtained. Especially, when the molar ratio of Ba in the
raw material solution is 1.3 ≦ x ≦ 1.7, Ic value can be improved remarkably compared
with the case of making the molar ratio of Ba into the standard molar ratio.
[0065] The above-mentioned result makes it reason that the property of the grain boundary
gives Jc (Ic value) big influence in addition to the degree of in-plane orientation
of the crystal of the superconducting layer and the degree of orientation of the crystal
direction in the a-b face.
[0066] That is, when the data of embodiment 1 (Y : Ba : Cu = 1 : 1.5 : 3) and comparative
example 1 (Y : Ba : Cu = 1 : 2 : 3, standard composition) is compared, Δφ and Δω are
comparable level, and the degree of in-plane orientation of the crystal and the degree
of orientation of the crystal direction in the a-b face do not have so much difference.
However, because Jc is 3.20 MA/cm
2 (Ic = 525A/cm) in embodiment 1 and is 2.58 MA/cm
2 (Ic = 307A/cm) in comparative example 1, there is a big difference. In comparative
example 1, this is considered as a result that the electric connectivity among the
crystal grains deteriorates by the precipitation of the impurities and the generation
of the cracks based on extra Ba in the grain boundaries of the crystal grains of the
Y (123) superconductor.
Therefore, as the molar ratio of Ba becomes higher like the comparative example 2
(molar ratio of Ba = 2.2) and the comparative example 3 (molar ratio of Ba = 2.5),
Jc deteriorates rapidly.
[0067] As mentioned above, according to this invention, it is possible to bring the Jc of
YBCO superconducting layer close to the Jc of inside of YBCO crystal, and Ic value
depending on the film thickness can be improved.
INDUSTRIAL APPLICABILITY
[0068] It is possible to thicken the film of the superconductor by this invention, the tape-shaped
Re-type (123) superconductor having high Ic value can be produced easily, and the
superconducting layer is formed by MOD process which is non-vacuum process. Therefore,
it is suitable to the long wire, and the production cost can be decreased remarkably.